Linked Data
dbSNP Id:
rs373730068
ExAC:
6:32149143 C / T
gnomAD v2:
6-32149143-C-T
gnomAD v3:
6-32181366-C-T
gnomAD v4:
6-32181366-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32181366C>T , CM000668.2:g.32181366C>T | GRCh38 |
| NC_000006.11:g.32149143C>T , CM000668.1:g.32149143C>T | GRCh37 |
| NC_000006.10:g.32257121C>T | NCBI36 |
| NG_029868.1:g.7957G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375076.9:c.1103G>A MANE Select | ENSP00000364217.4:p.Arg368His | |
| ENST00000375055.6:c.*30-127G>A | ENSP00000364195.2:n.*30-127G>A | |
| ENST00000375065.6:c.290G>A | ENSP00000364206.6:p.Arg97His | |
| ENST00000375067.7:c.948G>A | ENSP00000364208.3:p.Thr316= | |
| ENST00000375069.7:c.1151G>A | ENSP00000364210.4:p.Arg384His | |
| ENST00000375070.7:c.773G>A | ENSP00000364211.4:p.Arg258His | |
| ENST00000375076.8:c.1103G>A | ENSP00000364217.4:p.Arg368His | |
| ENST00000438221.6:c.*30-127G>A | ENSP00000387887.2:n.*30-127G>A | |
| ENST00000469940.5:n.270G>A | ||
| ENST00000473619.5:n.645G>A | ||
| ENST00000484849.5:n.1310G>A | ||
| ENST00000488669.5:n.616-127G>A | ||
| ENST00000620802.4:c.350G>A | ENSP00000484081.1:p.Arg117His | |
| NM_001136.4:c.1103G>A | NP_001127.1:p.Arg368His | |
| NM_001206929.1:c.1151G>A | NP_001193858.1:p.Arg384His | |
| NM_001206932.1:c.1061G>A | NP_001193861.1:p.Arg354His | |
| NM_001206934.1:c.*30-127G>A | NP_001193863.1:n.*30-127G>A | |
| NM_001206936.1:c.1022-127G>A | NP_001193865.1:n.1022-127G>A | |
| NM_001206940.1:c.*30-127G>A | NP_001193869.1:n.*30-127G>A | |
| NM_001206954.1:c.932-127G>A | NP_001193883.1:n.932-127G>A | |
| NM_001206966.1:c.*29+158G>A | NP_001193895.1:n.*29+158G>A | |
| NM_172197.2:c.948G>A | NP_751947.1:p.Thr316= | |
| NR_038190.1:n.1386G>A | ||
| XM_017010328.2:c.1073-127G>A | XP_016865817.1:n.1073-127G>A | |
| XR_001743189.2:n.1167G>A | ||
| XR_001743190.2:n.1119G>A | ||
| NM_001136.5:c.1103G>A MANE Select | NP_001127.1:p.Arg368His | |
| NM_001206932.2:c.1061G>A | NP_001193861.1:p.Arg354His | |
| NM_001206936.2:c.1022-127G>A | NP_001193865.1:n.1022-127G>A | |
| NM_001206940.2:c.*30-127G>A | NP_001193869.1:n.*30-127G>A | |
| NM_001206954.2:c.932-127G>A | NP_001193883.1:n.932-127G>A | |
| NM_001206966.2:c.*29+158G>A | NP_001193895.1:n.*29+158G>A | |
| NM_172197.3:c.948G>A | NP_751947.1:p.Thr316= | |
| NR_038190.2:n.1317G>A | ||
| NM_001206929.2:c.1151G>A | NP_001193858.1:p.Arg384His | |
| NM_001206934.2:c.*30-127G>A | NP_001193863.1:n.*30-127G>A |